Crynodeb
Purified M1 muscarinic cholinergic receptor and Gq/11 were coreconstituted in lipid vesicles. Addition of purified phospholipase C-beta 1 (PLC-beta 1) further stimulated the receptor-promoted steady-state GTPase activity of Gq/11 up to 20-fold. Stimulation depended upon receptor-mediated GTP-GDP exchange. Addition of PLC-beta 1 caused a rapid burst of hydrolysis of Gq/11-bound GTP that was at least 50-fold faster than in its absence. Thus, PLC-beta 1 stimulates hydrolysis of Gq/11-bound GTP and acts as a GTPase-activating protein (GAP) for its physiologic regulator, Gq/11. GTPase-stimulating activity was specific both for PLC-beta 1 and Gq/11. Such GAP activity by an effector coupled to a trimeric G protein can reconcile slow GTP hydrolysis by pure G proteins in vitro with fast physiologic deactivation of G protein-mediated signaling.
| Iaith wreiddiol | Saesneg |
|---|---|
| Tudalennau (o-i) | 411-418 |
| Nifer y tudalennau | 8 |
| Cyfnodolyn | Cell |
| Cyfrol | 70 |
| Rhif cyhoeddi | 3 |
| Dynodwyr Gwrthrych Digidol (DOIs) | |
| Statws | Cyhoeddwyd - 7 Awst 1992 |
| Cyhoeddwyd yn allanol | Ie |
Ôl bys
Gweld gwybodaeth am bynciau ymchwil 'Phospholipase C-beta 1 is a GTPase-activating protein for Gq/11, its physiologic regulator'. Gyda’i gilydd, maen nhw’n ffurfio ôl bys unigryw.Dyfynnu hyn
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